Scientific name	Authority	First published in
Discopodium penninervium var. holstii	(Dammer) Bitter	Bot. Jahrb. Syst. 57: 17. 1920.
Discopodium penninervium var. intermedium	Bitter	Bot. Jahrb. Syst. 57: 17. 1920.
Discopodium penninervium var. magnifolium	Chiov.	Nuovo Giorn. Bot. Ital. 36: 367. 1929.
Discopodium penninervium var. nervisequum	Bitter	Bot. Jahrb. Syst. 57: 17. 1920.
Discopodium penninervium var. sparsearaneosum	Bitter	Bot. Jahrb. Syst. 57: 17. 1920.
Solanum albersii	Damm. ex Bitter	Bot. Jahrb. Syst. 57(1): 16. 1920
Solanum cosmeticum	Delile	Sec. Voy. Choa [Rochet] 340. 1846.
Withania holstii	Dammer	Pflanzenw. Ost-Afrikas C (Engler): 351. 1895.

Common names Top

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Language	Common/alternative name
Amharic	ኣመራሮ

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Northeast Tropical Africa
  - Eritrea
  - Ethiopia
  - Sudan
- South Tropical Africa
  - Malawi
  - Mozambique
- West Tropical Africa
  - Benin
  - Nigeria
- West-central Tropical Africa
  - Burundi
  - Cameroon
  - Gulf Of Guinea Islands
  - Rwanda
  - Zaïre

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001021443
Tropicos	29605136
KEW	urn:lsid:ipni.org:names:815647-1
The Plant List	kew-2772978
Open Tree Of Life	694252
NCBI Taxonomy	481609
IUCN Red List	153945870
IPNI	815647-1
iNaturalist	716451
GBIF	5580905
EOL	5791603

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Plant species diversity, plant use, and classification of agroforestry homegardens in southern and southwestern Ethiopia

Kassa G, Bekele T, Demissew S, Abebe T

Heliyon

25-May-2023

PMCID:	PMC10241864
doi:	10.1016/j.heliyon.2023.e16341
PMID:	37287606

Woody species diversity and regeneration status of Sub-Alpine forest of Mount Adama exclosure site, Northwestern highlands of Ethiopia

Mengistu DA, Bekele DA, Gela AG, Meshesha DT, Getahun MM

Heliyon

20-May-2023

PMCID:	PMC10220367
doi:	10.1016/j.heliyon.2023.e16473
PMID:	37251442

Species Diversity, Structure, and Regeneration Status of Woody Plants in Saleda Yohans Church Forest, South Wollo, Ethiopia

Mekonnen AB, Mohammed AS, Demissew A

Scientifica (Cairo)

17-Apr-2023

PMCID:	PMC10125748
doi:	10.1155/2023/3853463
PMID:	37101718

Ethnobotanical study of endemic and non-endemic medicinal plants used by indigenous people in environs of Gullele botanical garden Addis Ababa, central Ethiopia: A major focus on Asteraceae family

Woldeamanuel MM, Geda MK, Mohapatra S, Bastia TK, Rath P, Panda AK

Front Pharmacol

23-Nov-2022

PMCID:	PMC9727095
doi:	10.3389/fphar.2022.1020097
PMID:	36506590

Antibacterial activity of medicinal plants in Indonesia on Streptococcus pneumoniae

Tafroji W, Margyaningsih NI, Khoeri MM, Paramaiswari WT, Winarti Y, Salsabila K, Putri HF, Siregar NC, Soebandrio A, Safari D

PLoS One

13-Sep-2022

PMCID:	PMC9469987
doi:	10.1371/journal.pone.0274174
PMID:	36099236

Antioxidant Activity and Anti-Nutritional Factors of Selected Wild Edible Plants Collected from Northeastern Ethiopia

Adamu E, Asfaw Z, Demissew S, Baye K

Foods

01-Aug-2022

PMCID:	PMC9368519
doi:	10.3390/foods11152291
PMID:	35954058

Medicinal Plants Used to Treat Human and Livestock Ailments in Basona Werana District, North Shewa Zone, Amhara Region, Ethiopia

Megersa M, Tamrat N

Evid Based Complement Alternat Med

14-Apr-2022

PMCID:	PMC9023155
doi:	10.1155/2022/5242033
PMID:	35463078

Traditional and Phytochemical Bases of Herbs, Shrubs, Climbers, and Trees from Ethiopia for Their Anticancer Response

Abate L, Tadesse MG, Bachheti A, Bachheti RK

Biomed Res Int

03-Feb-2022

PMCID:	PMC8831057
doi:	10.1155/2022/1589877
PMID:	35155671

Differences in Nectar Traits between Ornithophilous and Entomophilous Plants on Mount Cameroon

Janeček Š, Chmel K, Ewome FL, Hrubá K, Klomberg Y, Kobe IN, Kouede RD, Mertens JE, Njie MM, Tropek R

Plants (Basel)

08-Jun-2021

PMCID:	PMC8226534
doi:	10.3390/plants10061161
PMID:	34200999

Evaluation of Antibacterial Activity of Essential Oils and Their Combination against Multidrug-Resistant Bacteria Isolated from Skin Ulcer

Gadisa E, Usman H

Int J Microbiol

26-Mar-2021

PMCID:	PMC8019382
doi:	10.1155/2021/6680668
PMID:	33854550

Antimicrobial activities evaluation and phytochemical screening of some selected medicinal plants: A possible alternative in the treatment of multidrug-resistant microbes

Kebede T, Gadisa E, Tufa A

PLoS One

26-Mar-2021

PMCID:	PMC7997013
doi:	10.1371/journal.pone.0249253
PMID:	33770121

Relationships between topographic factors, soil and plant communities in a dry Afromontane forest patches of Northwestern Ethiopia

Birhanu L, Bekele T, Tesfaw B, Demissew S

PLoS One

12-Mar-2021

PMCID:	PMC7954303
doi:	10.1371/journal.pone.0247966
PMID:	33711027

Antimicrobial activity of medicinal plants used for urinary tract infections in pastoralist community in Ethiopia

Gadisa E, Tadesse E

BMC Complement Med Ther

23-Feb-2021

PMCID:	PMC7903779
doi:	10.1186/s12906-021-03249-7
PMID:	33622320

Ethnobotanical Study of Medicinal Plants Used by Traditional Healers to Treat Cancer-Like Symptoms in Eleven Districts, Ethiopia

Tesfaye S, Belete A, Engidawork E, Gedif T, Asres K

Evid Based Complement Alternat Med

21-Apr-2020

PMCID:	PMC7191438
doi:	10.1155/2020/7683450
PMID:	32382303

Impact of altitude and anthropogenic disturbance on plant species composition, diversity, and structure at the Wof-Washa highlands of Ethiopia

Yirga F, Marie M, Kassa S, Haile M

Heliyon

12-Aug-2019

PMCID:	PMC6702390
doi:	10.1016/j.heliyon.2019.e02284
PMID:	31453405

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
(+/-)-9-Hydroxyoctadeca-10E,12Z,dienoic acid	134689021	Click to see CCCCCC=CC=CC(CCCCCCCC(=O)O)O	296.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.001
9R-hydroxy-10E,12Z-octadecadienoic acid	16061059	Click to see CCCCCC=CC=CC(CCCCCCCC(=O)O)O	296.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.001
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
1,4-dihydroxy-7,9a-dimethyl-6-methylidene-4,5,5a,7,8,9-hexahydro-1H-benzo[e][2]benzofuran-3-one	74819448	Click to see CC1CCC2(C(C1=C)CC(C3=C2C(OC3=O)O)O)C	264.32	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.001
7alpha,11alpha-Dihydroxy-4(13),8-coloratadien-12,11-olide	42608152	Click to see CC1CCC2(C(C1=C)CC(C3=C2C(OC3=O)O)O)C	264.32	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.001
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(1S,2R,7S,9R,11S,12S,15S,16S)-15-hydroxy-15-[(1R,4R,5R,7R)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	162861518	Click to see CC12CCC3C(C1CCC2(C4CC5(CC4OC(=O)C5(C)O)C)O)CC6C7(C3(C(=O)C=CC7)C)O6	470.60	unknown	https://doi.org/10.1021/NP990446X
(1S,2R,7S,9R,11S,12S,15S,16S)-15-hydroxy-15-[(1R,4R,5R,7S)-4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	21603476	Click to see CC12CCC3C(C1CCC2(C4CC5(CC4OC(=O)C5(C)O)C)O)CC6C7(C3(C(=O)C=CC7)C)O6	470.60	unknown	https://doi.org/10.1021/NP990446X
9-Hydroxy-9-(4-hydroxy-4,5-dimethyl-3-oxo-2-oxabicyclo[3.2.1]oct-7-yl)-9a,11b-dimethyl-5a,6,6a,6b,7,8,9,9a,10,11,11a,11b-dodecahydrocyclopenta[1,2]phenanthro[8a,9-b]oxiren-1(4H)-one	495800	Click to see CC12CCC3C(C1CCC2(C4CC5(CC4OC(=O)C5(C)O)C)O)CC6C7(C3(C(=O)C=CC7)C)O6	470.60	unknown	https://doi.org/10.1021/NP990446X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(1S,2R,7S,9R,11S,12S,15R,16S)-15-hydroxy-15-[(1R,4R,5R,7S)-4-hydroxy-4,5,7-trimethyl-3-oxo-2-oxabicyclo[3.2.1]octan-7-yl]-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	101027516	Click to see CC12CCC3C(C1CCC2(C4(CC5(CC4OC(=O)C5(C)O)C)C)O)CC6C7(C3(C(=O)C=CC7)C)O6	484.60	unknown	https://doi.org/10.1021/NP990446X
(1S,2R,7S,9R,11S,12S,15S,16S)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-15-hydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	10095500	Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6)C)O5)C)O)C	454.60	unknown	https://doi.org/10.1016/0031-9422(93)85363-V
(1S,2S,4S,5R,10R,11S,13S,14R,15S,18S)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-5,13,15-trihydroxy-10,14-dimethyl-3-oxapentacyclo[9.7.0.02,4.05,10.014,18]octadec-7-en-9-one	163000243	Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3C2(C(CC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)O)C)O)C	486.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.001
(1S,2S,4S,5R,10R,11S,14S,15R,18S)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-5,15-dihydroxy-10,14-dimethyl-3-oxapentacyclo[9.7.0.02,4.05,10.014,18]octadec-7-en-9-one	101942518	Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3C2(CCC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)C)O)C	470.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.001 https://doi.org/10.1055/S-2006-957426
(3S,4R,6R)-6-[(1S)-1-[(5R,8S,9S,10S,13R,14S,17R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]ethyl]-3,4-dimethyloxan-2-one	154497687	Click to see CC1CC(OC(=O)C1C)C(C)C2CCC3C2(CCC4C3CCC5C4(CCCC5)C)C	414.70	unknown	https://doi.org/10.1021/NP990446X
[(1S,2R,7S,9R,11S,12S,14R,15R,16S)-15-[(1S)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-2,16-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-14-yl] acetate	10413503	Click to see CC1=C(C(=O)OC(C1)C(C)C2C(CC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6)C)O5)C)OC(=O)C)C	496.60	unknown	https://doi.org/10.1016/0031-9422(93)85363-V
[(1S,2R,7S,9R,11S,12S,14R,15S,16S)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-15-hydroxy-2,16-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-14-yl] acetate	102065718	Click to see CC1=C(C(=O)OC(C1)C(C)C2(C(CC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6)C)O5)C)OC(=O)C)O)C	512.60	unknown	https://doi.org/10.1016/0031-9422(93)85363-V
[15-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-15-hydroxy-2,16-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-14-yl] acetate	163028823	Click to see CC1=C(C(=O)OC(C1)C(C)C2(C(CC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6)C)O5)C)OC(=O)C)O)C	512.60	unknown	https://doi.org/10.1016/0031-9422(93)85363-V
[15-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-2,16-dimethyl-3-oxo-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-14-yl] acetate	85136124	Click to see CC1=C(C(=O)OC(C1)C(C)C2C(CC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6)C)O5)C)OC(=O)C)C	496.60	unknown	https://doi.org/10.1016/0031-9422(93)85363-V
15-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-15-hydroxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadec-4-en-3-one	162910374	Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6)C)O5)C)O)C	454.60	unknown	https://doi.org/10.1016/0031-9422(93)85363-V
15-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-5,13,15-trihydroxy-10,14-dimethyl-3-oxapentacyclo[9.7.0.02,4.05,10.014,18]octadec-7-en-9-one	74323736	Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3C2(C(CC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)O)C)O)C	486.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.001
15-[1-(4,5-dimethyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)-1-hydroxyethyl]-5-hydroxy-10,14-dimethyl-3-oxapentacyclo[9.7.0.0^{2,4}.0^{5,10}.0^{14,18}]octadec-7-en-9-one	14236710	Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)C)O)C	470.60	unknown	https://doi.org/10.1055/S-2006-957426
CID 301757	301757	Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3C2(CCC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)C)O)C	470.60	unknown	https://doi.org/10.1055/S-2006-957426 https://doi.org/10.1016/J.PHYTOCHEM.2007.11.001
jaborosalactone L	44566997	Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6)CO)O5)C)O)C	470.60	unknown	https://doi.org/10.1016/0031-9422(93)85363-V
Withanolide A	11294368	Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)C)O)C	470.60	unknown	https://doi.org/10.1055/S-2006-957426
Withanone	21679027	Click to see CC1=C(C(=O)OC(C1)C(C)C2(CCC3C2(CCC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)C)O)C	470.60	unknown	https://doi.org/10.1055/S-2006-957426 https://doi.org/10.1016/J.PHYTOCHEM.2007.11.001
> Organoheterocyclic compounds / Azoles / Pyrazoles / Phenylpyrazoles
Withasomnine	442877	Click to see C1CC2=C(C=NN2C1)C3=CC=CC=C3	184.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.001
> Organoheterocyclic compounds / Naphthofurans
(1R,4R,5aS,9aS)-1,4-dihydroxy-6,6,9a-trimethyl-4,5,5a,7,8,9-hexahydro-1H-benzo[e][2]benzofuran-3-one	10945374	Click to see CC1(CCCC2(C1CC(C3=C2C(OC3=O)O)O)C)C	266.33	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.001
1,4-dihydroxy-6,6,9a-trimethyl-4,5,5a,7,8,9-hexahydro-1H-benzo[e][2]benzofuran-3-one	45783127	Click to see CC1(CCCC2(C1CC(C3=C2C(OC3=O)O)O)C)C	266.33	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.11.001

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Discopodium penninervium

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top